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NCT05853926 Clinical Trial

Spinal Manipulation With Laser Therapy Versus Dry Needling in Chronic Lower Backache

Low Back Pain Clinical Trial

Official title:
Spinal Manipulation With Laser Therapy Versus Dry Needling in Chronic Lower Backache: Randomized Controlled Trial

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05853926
Other study ID # DPT/Batch-Fall18/530
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 1, 2023
Est. completion date August 31, 2023

Study information
Verified date May 2023
Source Superior University
Contact Kausar Kalsoom
Phone +923081841078
Email kausarkalsoom832@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To determine the effectiveness of spinal manipulation with laser therapy versus dry needling for pain, disability and fear of movement in chronic low backache

Recruitment information / eligibility
Status Recruiting
Enrollment 54
Est. completion date August 31, 2023
Est. primary completion date June 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - Those patients will be included in the study who have chronic low back pain (12 week duration). both genders aged 18-60 years low back pain Exclusion Criteria: - Those patients will be excluded in the study who have needle phobia, any infection, cancer, dermal changings, heart transplant, pregnancy, rheumatic fever(25)fracture, cauda equina syndrome, arrhythmia, sensory deficiency, mental illness, surgery, osteoporosis, low term use of steroid

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• Spinal Manipulation With Laser Therapy
Spinal Manipulation With Laser Therapy in Chronic Lower Backache
• Dry Needling
Dry Needling in Chronic Lower Backache

Locations
Country Name City State
Pakistan Chaudary Muhammad Akram Teaching Hospital Lahore Punjab

Sponsors (1)
Lead Sponsor Collaborator
Superior University

Country where clinical trial is conducted

Pakistan, 

Outcome
Type Measure Description Time frame Safety issue
Primary Oswestry Disability Index scale 6 Months
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